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of the Project Manager Execute each project phase as defined in PMO methodology and project RACIs Translate business scope into project workstreams to enable outcomes Work with SMEs and external PMs to organize and plan projects for success Manage day to day integrated dependencies and milestones for project plan Identify, assess, and mitigate risks and issues that can dis
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of the Senior Business Analyst/Process Analyst Document current as is process and gap analysis around product serialization Heavy focus on execution, but there will be strategic components and developing alternative plans Build out a baseline for serialization and use cases for potential approaches to solve challenges Collaborate extensively with Senior Project Manager and
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Our Life Sciences Client is seeking a strong Project Manager to support operational projects within an enterprise R&D PMO. You will support enterprise project management and help set up a SharePoint site; experience implementing SharePoint is a must! We can facilitate w2 and corp to corp consultants. For our w2 consultants, we offer a great benefits package that includes
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of the Electrical Engineer Maintain electronic designs for surgical equipment Create proper documentation outlining the alternative and redesign of PC boards Perform electrical and mechanical design testing, perform product functional analysis and root cause analysis Provide input into the creation of technical documents including technical specifications and design failur
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of the Senior Electrical Engineer Analyze, design, implement, document, and model closed loop control systems Perform in depth analysis of electrical and software systems for stability under varying environmental and power conditions Analyze, design, implement, document, and model mathematical solutions for control electronic subsystems Lead efforts to generate product req
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We have an excellent job opportunity as a Digital Quality Lead with our leading biopharma client. In this role you will oversee quality of implementation projects and ensure the quality and compliance of all GxP activities. Our role is expected to last 6 12 months. Requirements of the Digital Quality Lead Bachelor's degree in IT, Life Sciences, Chemistry, Engineering, or
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of the Senior QA/RA Consultant Advise entire team on MDR process Review data flows, risk assessments, and gap assessments of current QMS for the new MDR implementation Improve process based on previous MDR implementation, previous work with Notified Bodies Determine gaps within the Quality System, Post Market Report System, Quality and Clinical Teams Review with team membe
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We have an excellent job opportunity as a Digital Quality Lead with our leading biopharma client. In this role you will oversee quality of implementation projects and ensure the quality and compliance of all GxP activities. Our role is expected to last 6 12 months. Requirements of the Digital Quality Lead Bachelor's degree in IT, Life Sciences, Chemistry, Engineering, or
Posted Today
of the Post Market Surveillance Writer Provide leadership and direction to PMS staff Ensure compliance with domestic and international regulations and requirements Help develop and monitor adherence to schedules for PMS reports Produce PMS documentation such as PMSPs and PSURs Act as point of contact for internal customers Job ID 369360 About EG Life Sciences Founded in 20
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of the Equipment Validation Consultant Revalidate process equipment Requalify CTUs Requalify critical utility systems Perform air flow visualization smoke studies Support equipment/utilities validations Support shipping studies Work across teams and functions Job ID 369009 About EG Life Sciences Founded in 2010, EG Life Sciences is a national professional services firm tha
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100% Remote We have an excellent job opportunity available as a remote Project Manager! Our role is expected to last 12 months. Responsibilities of the Project Manager Coordinate activities within assigned projects, ensuring alignment with organizational objectives Help define project scope and deliverables, milestones and timelines, project risks and contingency plans Tr
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of the Biologics CMC Writer Draft and edit CMC drug product "P" sections of regulatory documents for submission to regulatory agencies worldwide Work with SMEs to write and edit SOPs, specifications, batch documentation, and related Work closely with technical operations team to ensure alignment and established priorities Collaborate with QA and regulatory affairs teams to
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of the Biologics CMC Writer Draft and edit CMC drug product "S" sections of regulatory documents for submission to regulatory agencies worldwide Work with SMEs to write and edit SOPs, specifications, batch documentation, and related Work closely with technical operations team to ensure alignment and established priorities Collaborate with QA and regulatory affairs teams to
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of the Clinical Quality Consultant SOP review and evaluation within study/data/vendor/medical management, site monitoring, statistical programming, QMS Perform risk assessment of SOP adoption Provide recommendations on adoption Offer SOP training for relevant teams Requirements of the Clinical Quality Consultant Bachelor's degree Strong GCP deep clinical quality experience
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100% Remote or onsite in Tampa at candidate's preference Our Fortune 500 pharma client needs a Senior Regulatory Affairs Consultant to support an influx of work around submissions and change controls for their Cell & Gene Therapy products. Contract Length 12 months, with the possibility of extension/conversion Requirements of the Senior Regulatory Affairs Consultant Bache
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